1 Preparation issuance and review of
SOP / Guidelines
FP Specifications / Standard Test Procedures
Analytical documents
PM Specifications / STP
General Testing Procedures (GTP)
2 Generation of item / product codes
3 Compilation and storage of documents for product registrations
4 Review of production record / Record of Analysis to assess that no errors have occurred and
the records are complete and accurate. If errors have occurred, responsible to assure that
the errors have been fully investigated. Retention and storage of the records.
5 Review and approval / rejection of any change to procedure(s), process, specifications,
equipment, facility, production and laboratory controls and other(s).
6 Issuance, control, review and retrieval of all controlled Logbooks / registers, records, SOP,
SCP, STP, FPS etc. Their retention and storage.
7 Ensuring of validation and qualification activity. Qualification and validation documentation.
8 Maintaining liaisons with local FDA and maintain records.
9 Preparation and review of technical documents like VMP & SMF.
10 Continuous training at site for document management.
Interested Candidates can share their resumes on sh**********a@wa***********l.com
Martin & Harris Pvt Ltd a reputed Pharmaceutical company of Apeejay Stya Group incorporated in 1924 under the Companies Act, 1956 actively engaged in providing Third Party (3PL) solutions for the pharmaceutical sector in India. The company has unique distinction of having a nationwide IT-enabled...